Mutation in ε-Sarcoglycan Induces a Myoclonus-Dystonia Syndrome-Like Movement Disorder in Mice

Myoclonus dystonia syndrome (MDS) is an inherited movement disorder, and most MDS-related mutations have so far been found in the ε-sarcoglycan (SGCE) coding gene. By generating SGCE-knockout (KO) and human 237 C > T mutation knock-in (KI) mice, we showed here that both KO and KI mice exerted typ...

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Detalhes bibliográficos
Publicado no:Neurosci Bull
Main Authors: Li, Jiao, Liu, Yiqiong, Li, Qin, Huang, Xiaolin, Zhou, Dingxi, Xu, Hanjian, Zhao, Feng, Mi, Xiaoxiao, Wang, Ruoxu, Jia, Fan, Xu, Fuqiang, Yang, Jing, Liu, Dong, Deng, Xuliang, Zhang, Yan
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Singapore 2020
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7954997/
https://ncbi.nlm.nih.gov/pubmed/33355901
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12264-020-00612-5
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